Potassium Cation → 5-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one

HRID 690344Notes

Reaction equation

HRID 690344 reaction equation
[Br:13][c:14]1[c:15]([CH2:21][Br:22])[cH:16][c:17]([Cl:20])[cH:18][cH:19]1.[C:23](=[O:24])([O-:25])[O-:26].[CH3:29][N:30]([CH3:31])[CH:32]=[O:33].[CH3:34][CH2:35][O:36][C:37](=[O:38])[CH3:39].[K+:27].[K+:28].[OH:1][c:2]1[c:3]2[c:8]([cH:9][cH:10][cH:11]1)[C:7](=[O:12])[CH2:6][CH2:5][CH2:4]2>>[O:1]([c:2]1[c:3]2[c:8]([cH:9][cH:10][cH:11]1)[C:7](=[O:12])[CH2:6][CH2:5][CH2:4]2)[CH2:21][c:15]1[c:14]([Br:13])[cH:19][cH:18][c:17]([Cl:20])[cH:16]1

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 1199215-Hydroxy-1-tetraloneHCID 118465052-Bromo-5-chlorobenzyl bromide

Product 1

HCID 696731795-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one

Sources & evidence

ORD record
ord-07cffc8f4273476c89bac3010e15d9df
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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